Zobrazeno 1 - 10
of 142
pro vyhledávání: '"Eli, Hershkovitz"'
Autor:
Eli Hershkovitz, David Strich
Publikováno v:
Frontiers in Endocrinology, Vol 14 (2023)
Externí odkaz:
https://doaj.org/article/11bfeeb31f404fbfa3e399f78d05e302
Autor:
David Shaki, Marina Eskin-Schwartz, Noam Hadar, Emily Bosin, Lior Carmon, Samuel Refetoff, Eli Hershkovitz, Ohad S Birk, Alon Haim
Publikováno v:
European Thyroid Journal, Vol 11, Iss 1, Pp 1-6 (2023)
Objective: Bi-allelic loss-of-function mutations in TSHB, encoding the beta subunit of thyroid-stimulating hormone (TSH), cause congenital hypothyroidism. Homozygosity for the TSHB p.R75G variant, previously described in South Asian individuals, does
Externí odkaz:
https://doaj.org/article/4d2799ea23084429a95d73bf5e191201
Autor:
Isaac Lazar, Dorit Wizeman-Orlov, Guy Hazan, Asaf Orbach, Alon Haim, Yuval Cavari, Yael Feinstein, Eitan Neeman, Eli Hershkovitz, Yaniv Faingelernt
Publikováno v:
Frontiers in Pediatrics, Vol 11 (2023)
IntroductionOur aims were to determine whether anion gap normalization time (AGNT) correlates with risk factors related to the severity of diabetic ketoacidosis (DKA) in children, and to characterize AGNT as a criterion for DKA resolution in children
Externí odkaz:
https://doaj.org/article/4d427a914ba648c8ba0d54cf5e8b1aa9
Autor:
David Shaki, Eli Hershkovitz, Shai Tamam, Arkadi Bollotin, Odeya David, Guy Yalovitsky, Neta Loewenthal, Lior Carmon, Dganit Walker, Raphael Nowak, Alon Haim
Publikováno v:
Frontiers in Endocrinology, Vol 14 (2023)
ObjectiveTo analyze and determine the safety and efficacy of growth hormone (GH) treatment in Down syndrome (DS) pediatric patients and to weigh ethical aspects involved.DesignSystematic review and mini meta-analysis of the literature.MethodsA search
Externí odkaz:
https://doaj.org/article/2f0df266defd4aec8f9e6135fe844826
Autor:
Orna Staretz-Chacham, Nadirah S. Damseh, Suha Daas, Nasser Abu Salah, Yair Anikster, Ortal Barel, Elena Dumin, Aviva Fattal-Valevski, Tzipora C. Falik-Zaccai, Eli Hershkovitz, Sagi Josefsberg, Yuval Landau, Tally Lerman-Sagie, Hanna Mandel, Rachel Rock, Nira Rostami, Talya Saraf-Levy, Nava Shaul Lotan, Ronen Spiegel, Galit Tal, Igor Ulanovsky, Yael Wilnai, Stanley H. Korman, Shlomo Almashanu
Publikováno v:
Frontiers in Genetics, Vol 14 (2023)
Introduction: Hereditary orotic aciduria is an extremely rare, autosomal recessive disease caused by deficiency of uridine monophosphate synthase. Untreated, affected individuals may develop refractory megaloblastic anemia, neurodevelopmental disabil
Externí odkaz:
https://doaj.org/article/a4eeec32a8884c4395e424f817425fe1
Autor:
David Shaki, Eli Hershkovitz, Shai Tamam, Arkadi Bollotin, Odeya David, Guy Yalovitsky, Neta Loewenthal, Lior Carmon, Dganit Walker, Alon Haim
Publikováno v:
Frontiers in Pediatrics, Vol 11 (2023)
ObjectiveTo analyze and determine the quality of functioning in different components of GHRH-GH-IGF1 axis in children with Down syndrome (DS).DesignSystematic review and mini meta-analysis of the literature.MethodsA search was performed in PubMed, Em
Externí odkaz:
https://doaj.org/article/61d8dbe44d384a81aa1f825a34e94702
Autor:
Eyal Kristal, Ben Pode-Shakked, Guy Hazan, Ehud Banne, Galina Ling, Odeya David, Eilon Shany, Annick Raas-Rothschild, Yair Anikster, Katya Kneller, Eli Hershkovitz, Yuval E. Landau, Ronen Spiegel, Yoav Zehavi, Orna Staretz-Chacham
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 16, Iss 1, Pp 1-6 (2021)
Abstract Background Severe acute respiratory syndrome coronavirus 2 (SARS CoV-2) is the causative agent of the current COVID-19 pandemic. Lysosomal storage disorders (LSD) comprise of 70 inherited inborn errors of metabolism. Affected individuals suf
Externí odkaz:
https://doaj.org/article/8b5cbfe869724833b439ca921dcf05fd
Autor:
Odeya David, Rotem Agur, Rosa Novoa, David Shaki, Dganit Walker, Lior Carmon, Marina Eskin-Schwartz, Ohad S. Birk, Galina Ling, Ruth Schreiber, Neta Loewenthal, Alon Haim, Eli Hershkovitz
Publikováno v:
Frontiers in Pediatrics, Vol 10 (2022)
BackgroundHypoparathyroidism, retardation, and dysmorphism (HRD) Syndrome is a rare disease composed of hypoparathyroidism, retardation of both growth and development, and distinctive dysmorphic features. Here, we describe the long-term morbidity and
Externí odkaz:
https://doaj.org/article/b919aa2daa0845d08495071b63ddbdb9
Autor:
Pierre Majdalani, Uri Yoel, Tayseer Nasasra, Merav Fraenkel, Alon Haim, Neta Loewenthal, Raz Zarivach, Eli Hershkovitz, Ruti Parvari
Publikováno v:
International Journal of Molecular Sciences, Vol 24, Iss 9, p 8233 (2023)
Familial non-medullary thyroid cancer (FNMTC) is a well-differentiated thyroid cancer (DTC) of follicular cell origin in two or more first-degree relatives. Patients typically demonstrate an autosomal dominant inheritance pattern with incomplete pene
Externí odkaz:
https://doaj.org/article/da900efa3a8a47378d78826a83e65d83
Publikováno v:
Frontiers in Pediatrics, Vol 10 (2022)
Carbon monoxide (CO) poisoning is a serious health problem. The main pathophysiological mechanism of acute CO poisoning is hypoxia due to the formation of carboxyhemoglobin (COHb). Delayed neuropsychiatric sequel (DNPS) occurs following an interval o
Externí odkaz:
https://doaj.org/article/9e4a3e1cafac46e29cefa684627765af